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Van Vlierberghe, M.

Publications and source records attributed to Van Vlierberghe, M..

3 recordsLinked to original sources

Out of Antarctica: new insights into Antarctic Subcluster 5.2 picocyanobacteria based on high-quality genomes

2.Synechococcus-like cyanobacteria are cosmopolitan unicellular picocyanobacteria that have colonized diverse aquatic and terrestrial habitats. The so-called subcluster 5.2 represents a particularly diversified subgroup, including marine and freshwater organisms adapted to extreme conditions, notably polar environments. We increased the genomic representation of polar taxa in this subcluster by reconstructing new high-quality genomes from five Antarctic lacustrine strains and one Arctic freshwater isolate using a combination of small Illumina and long Nanopore reads. A maximum likelihood (ML) phylogenomic analysis of these new assemblies combined with all publicly available good quality assemblies of the subcluster 5.2 suggests evidence of a dispersal process from Antarctica. Indeed, the topology of the phylogenomic tree indicates one basal Antarctic lineage followed by the emergence of two lineages, one Antarctic and one non-Antarctic (Spain). This finding is further supported by a 16S rRNA ML phylogenetic and a pangenomic analysis. Although secondary colonization of Antarctica by cyanobacteria following the cooling of the continent 34 million years ago has been reported, this study is the first to support an Out-of-Antarctica scenario inside subcluster 5.2. 3. Impact statementThis study provides novel insights into the evolutionary history and biogeography of Synechococcus-like picocyanobacteria. By expanding the genomic sampling of polar subcluster 5.2, we reveal that Antarctic taxa are not monophyletic and are intermixed with non-Antarctic lineages, suggesting an unprecedented Out-of-Antarctica dispersal scenario. Our results, supported by 16S rRNA, phylogenomic and pangenomic analyses, highlight the role of polar regions as both a refuge and a source of microbial diversity. This work advances our understanding of cyanobacterial adaptation, radiation and genome evolution in extreme environments. 4. Data summaryRaw sequencing reads and genome assemblies from this study have been deposited in the European Nucleotide Archive (ENA) under Project accession number PRJEB103944. Raw sequencing reads are available under accession numbers ERR15933635 to ERR15933638, ERR15933641 to ERR15933644, ERR15903357, ERR15903358, ERR15905256 and ERR15905257. The assemblies can be accessed under accession numbers GCA_977927515, GCA_977927525, GCA_977927535, GCA_977927545, GCA_977927555 and GCA_977929215. The scripts and code as well as large supplementary files generated during this study are available on Figshare and can be downloaded from https://doi.org/10.6084/m9.figshare.30772781 [1]. Supplementary data files are also provided and contains supplementary figures (Fig. S1-S4) and tables (Table S1-S6).

ecology↗

ToRQuEMaDA: Tool for Retrieving Queried Eubacteria, Metadata and Dereplicating Assemblies

TQMD is a tool which downloads, stores and produces lists of dereplicated prokaryotic genomes. It has been developed to counter the ever-growing number of prokaryotic genomes and their uneven taxonomic distribution. It is based on word-based alignment-free methods (k-mers), an iterative single-linkage approach and a divide-and-conquer strategy to remain both efficient and scalable. We studied the performance of TQMD by verifying the influence of its parameters and heuristics on the clustering outcome. We further compared TQMD to two other dereplication tools (dRep and Assembly-Dereplicator). Our results showed that TQMD is optimized to dereplicate at high taxonomic levels (phylum/class), whereas the other dereplication tools are optimized for lower taxonomic levels (species/strain), making TQMD complementary to the existing dereplicating tools. TQMD is available at .

bioinformatics↗

Consensus assessment of the contamination level of publicly available cyanobacterial genomes

BACKGROUNDPublicly available genomes are crucial for phylogenetic and metagenomic studies, in which contaminating sequences can be the cause of major problems. This issue is expected to be especially important for Cyanobacteria because axenic strains are notoriously difficult to obtain and keep in culture. Yet, despite their great scientific interest, no data are currently available concerning the quality of publicly available cyanobacterial genomes.\n\nRESULTSAs reliably detecting contaminants is a complex task, we designed a pipeline combining six methods in a consensus strategy to assess the contamination level of 440 genome assemblies of Cyanobacteria. Two methods are based on published reference databases of ribosomal genes (SSU rRNA 16S and ribosomal proteins), one is indirectly based on a reference database of marker genes (CheckM), and three are based on complete genome analysis. Among those genome-wide methods, Kraken and DIAMOND blastx share the same reference database that we derived from Ensembl Bacteria, whereas CONCOCT does not require any reference database, instead relying on differences in DNA tetramer frequencies. Given that all the six methods appear to have their own strengths and limitations, we used the consensus of their rankings to infer that >5% of cyanobacterial genome assemblies are highly contaminated by foreign DNA (i.e., contaminants were detected by 5 or 6 methods).\n\nCONCLUSIONSOur results will help researchers to check the quality of publicly available genomic data before use in their own analyses. Moreover, we argue that journals should make mandatory the submission of raw read data along with genome assemblies in order to facilitate the detection of contaminants in sequence databases.

genomics↗